Results 251 to 260 of about 1,116,836 (319)
Effects of citric acid and heat-treated soybean meal on rumen fermentation characteristics, methane emissions, and microbiota: an <i>in vitro</i> study. [PDF]
Yoo D, Oh J, Jeong S, Seo J.
europepmc +1 more source
The Comparative Value of Urea and Linseed Meal for Milk Production
I.W. Rupel, G. Bohstedt, E.B. Hart
openalex +1 more source
THE SECRETION OF GASTRIC MUCIN IN MAN. A COMPARATIVE STUDY IN THE NORMAL SUBJECT AND IN THE PATIENT WITH PEPTIC ULCER IN RESPONSE TO AN ALCOHOL TEST MEAL [PDF]
Richmond K. Anderson, Samuel J. Fogelson
openalex +1 more source
Abstract A combination of nucleotide hepatitis C virus (HCV) nonstructural protein (NS) 5B and 5A inhibitors is a preferred standard of care for treating chronic HCV. Bemnifosbuvir is a novel oral guanosine nucleotide prodrug with potent pan‐genotypic inhibitory activity against HCV NS5B.
Xiao‐Jian Zhou+7 more
wiley +1 more source
Contamination of aflatoxin B<sub>1</sub>, deoxynivalenol and zearalenone in feeds in China from 2021 to 2024. [PDF]
Liu M+10 more
europepmc +1 more source
Abstract This study (NCT04537715) investigated itraconazole (strong cytochrome P450 [CYP] 3A inhibitor) and rifampin (strong CYP3A inducer) on tazemetostat pharmacokinetics. In Part 1, patients received tazemetostat 400 mg orally on Days 1, 15, and 36, and 400 mg twice daily on Days 3‐14 and Days 21‐35.
Yingxue Chen+6 more
wiley +1 more source
The Use of Soybean Meal in the Diet of Growing Chicks
John C. Hammond, Harry W. Titus
openalex +1 more source
Abstract Valemetostat tosylate (valemetostat) is a dual inhibitor of enhancer of zeste homolog (EZH) 2 and EZH1, approved in Japan for the treatment of relapsed/refractory peripheral T‐cell lymphoma and adult T‐cell leukemia/lymphoma. This Phase I, open‐label study evaluated the pharmacokinetics and safety of a single 50‐mg oral dose of valemetostat in
Masaya Tachibana+8 more
wiley +1 more source
Daytime eating during simulated night work mitigates changes in cardiovascular risk factors: secondary analyses of a randomized controlled trial. [PDF]
Chellappa SL+6 more
europepmc +1 more source
Abstract This Phase 1 study of ubrogepant was conducted to establish the bioequivalence (BE) of the 50‐ and 100‐mg to‐be‐marketed (TBM) tablet formulations with the clinical trial (CT) 100‐mg tablet formulation and evaluate the food effect on the bioavailability of the 100‐mg TBM tablet. This 2‐part study enrolled healthy participants aged 18‐45 years.
Ramesh Boinpally, Joel M. Trugman
wiley +1 more source